HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221170Generated: October 27, 2026
Diethyl Ether → (7-bromo-9H-fluoren-2-yl)-dibutyl amine
https://huagongshe.com/reaction/221170
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-7-bromofluorene | HCID 23126 | — |
| Solvent | Water | HCID 962 | — |
| Product | (7-bromo-9H-fluoren-2-yl)-dibutyl amine | HCID 59325934 | — |
Reaction Steps
Under N2 atmosphere, 0.52 parts of 7-bromo-9H-fluoren-2-ylamine, 1.47 parts of 1-iodobutane, and 1.38 parts of potassium carbonate were added into 15 parts of dry dimethylformamide, followed by stirring and mixing. Then, the reaction mixture was heated to 120° C. and reacted for 24 hours. After the reaction mixture was cooled, poured the water into the reaction mixture for quenching the reaction, and using the diethyl ether to extract the product, and magnesium sulfate was used for dehydration. After removing the solvent, the residual was purified with column chromatography method by using dichloromethane/hexane co-solvent as an eluent, to obtain a compound (11) of the present example. This compound was in a form of a yellowish-brown solid, and the yield of this compound was 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08203068B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-e81505a9e7ea473390b60e2d3a1fefad |
|---|
| Source note | uspto-grants-2012_06 |
|---|